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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 976934생성일: 2026년 10월 24일

Ammonium Sulfate → 4-Amino-2-phenyl-8-[2-deoxy-3,5-di-O-(4-chlorobenzoyl)-beta-D-ribofuranosyl]-pteridine-7-one

https://huagongshe.com/ko/reaction/976934

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium SulfateHCID 6097028—
반응물alpha-D-erythro-Pentofuranosyl chloride, 2-deoxy-, 3,5-bis(4-chlorobenzoate)HCID 9845541—
반응물4-Amino-2-phenyl-pteridine-7-oneHCID 54402511—
촉매Silver perchlorateHCID 24562—
용매DichloromethaneHCID 6344—
용매HexamethyldisilazaneHCID 13838—
생성물4-Amino-2-phenyl-8-[2-deoxy-3,5-di-O-(4-chlorobenzoyl)-beta-D-ribofuranosyl]-pteridine-7-oneHCID 15403909—

반응 단계

A mixture of 1.0 g (4.2 mmol) of 4-amino-2-phenyl-pteridine-7-one (3) and a few crystals of ammonium sulfate was heated in 100 mL of hexamethyldisilazane (HMDS) under reflux for 4 hours. After cooling the excess HMDS was distilled off in vacuum and the residue dissolved in 100 mL of dry toluene. To the mixture was added 2.17 g (4.6 mmol) of 2-deoxy-3,5-di-O-(4-chlorobenzoyl)-α-D-ribofuranosyl chloride (made as in Example 3, step (a) for the toluyl derivative) and 0.476 g (2.3 mmol) of silver perchlorate. The solution was then stirred under anhydrous conditions for 24 hours at room temperature and then diluted with 200 mL of CH2Cl2. The resulting AgCl precipitate was filtered off through silica and then the filtrate was treated with 100 mL of a saturated aqueous solution of sodium bicarbonate followed by 100 mL of a saturated aqueous solution of NaCl. The organic layer was dried over Na2SO4, filtered and then the filtrate evaporated.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05612468
출처 데이터셋uspto-grants-1997_03
ORD IDord-e1b73d28aa304de09ead78bae0f1502b
출처 메모uspto-grants-1997_03